Recent advances in managing gastrointestinal stromal tumor

Florence Duffaud1,2,3, Axel Le Cesne4

  • 1Service d'Oncologie Médicale, CHU La Timone, Marseille, France.

F1000Research
|September 21, 2017
PubMed

Insights

Gastrointestinal stromal tumors (GISTs) are driven by mutations in KIT and PDGFRα. This review covers current pharmacotherapy for localized and metastatic GISTs, highlighting targeted kinase inhibitors.

Area of Science:

  • Oncology
  • Molecular Biology
  • Pharmacology

Background:

  • Gastrointestinal stromal tumors (GISTs) are primarily driven by activating mutations in receptor tyrosine kinases, specifically KIT and platelet-derived growth factor receptor alpha (PDGFRα).
  • GISTs represent a key model for understanding and targeting oncogenic kinase-driven cancers.
  • The precise understanding of GIST pathogenesis has led to the development of targeted therapies.

Purpose of the Study:

  • To review the current standard of care for pharmacotherapy in managing GISTs.
  • To discuss the role of targeted therapies in both localized and metastatic settings.
  • To provide an overview of treatment strategies for GIST patients.

Main Methods:

  • Literature review of current clinical guidelines and landmark studies.
  • Analysis of pharmacotherapeutic options for GIST management.
  • Synthesis of data on efficacy and safety of targeted agents.

Main Results:

  • Pharmacotherapy, particularly tyrosine kinase inhibitors, is the cornerstone of GIST management.
  • Targeted agents have significantly improved outcomes for patients with both localized and metastatic disease.
  • Treatment strategies are tailored based on mutation status, disease stage, and prior therapies.

Conclusions:

  • Targeted inhibition of KIT and PDGFRα has revolutionized GIST treatment.
  • Current pharmacotherapy offers effective options for localized and advanced GIST.
  • Ongoing research continues to refine treatment approaches for GIST patients.